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5JFO

Structure of the M.tuberculosis enoyl-reductase InhA in complex with GSK625

Functional Information from GO Data
ChainGOidnamespacecontents
A0004318molecular_functionenoyl-[acyl-carrier-protein] reductase (NADH) activity
A0005504molecular_functionfatty acid binding
A0005886cellular_componentplasma membrane
A0006633biological_processfatty acid biosynthetic process
A0009274cellular_componentpeptidoglycan-based cell wall
A0016491molecular_functionoxidoreductase activity
A0030497biological_processfatty acid elongation
A0046677biological_processresponse to antibiotic
A0050343molecular_functiontrans-2-enoyl-CoA reductase (NADH) activity
A0070403molecular_functionNAD+ binding
A0071768biological_processmycolic acid biosynthetic process
B0004318molecular_functionenoyl-[acyl-carrier-protein] reductase (NADH) activity
B0005504molecular_functionfatty acid binding
B0005886cellular_componentplasma membrane
B0006633biological_processfatty acid biosynthetic process
B0009274cellular_componentpeptidoglycan-based cell wall
B0016491molecular_functionoxidoreductase activity
B0030497biological_processfatty acid elongation
B0046677biological_processresponse to antibiotic
B0050343molecular_functiontrans-2-enoyl-CoA reductase (NADH) activity
B0070403molecular_functionNAD+ binding
B0071768biological_processmycolic acid biosynthetic process
C0004318molecular_functionenoyl-[acyl-carrier-protein] reductase (NADH) activity
C0005504molecular_functionfatty acid binding
C0005886cellular_componentplasma membrane
C0006633biological_processfatty acid biosynthetic process
C0009274cellular_componentpeptidoglycan-based cell wall
C0016491molecular_functionoxidoreductase activity
C0030497biological_processfatty acid elongation
C0046677biological_processresponse to antibiotic
C0050343molecular_functiontrans-2-enoyl-CoA reductase (NADH) activity
C0070403molecular_functionNAD+ binding
C0071768biological_processmycolic acid biosynthetic process
D0004318molecular_functionenoyl-[acyl-carrier-protein] reductase (NADH) activity
D0005504molecular_functionfatty acid binding
D0005886cellular_componentplasma membrane
D0006633biological_processfatty acid biosynthetic process
D0009274cellular_componentpeptidoglycan-based cell wall
D0016491molecular_functionoxidoreductase activity
D0030497biological_processfatty acid elongation
D0046677biological_processresponse to antibiotic
D0050343molecular_functiontrans-2-enoyl-CoA reductase (NADH) activity
D0070403molecular_functionNAD+ binding
D0071768biological_processmycolic acid biosynthetic process
Functional Information from PDB Data
site_idAC1
Number of Residues22
Detailsbinding site for residue NAD A 301
ChainResidue
AGLY14
ASER94
AILE95
AGLY96
AMET147
AASP148
APHE149
ALYS165
AALA191
APRO193
AILE194
AILE15
ATHR196
A6KA302
AHOH401
AILE16
ASER20
AILE21
APHE41
ALEU63
AASP64
AVAL65

site_idAC2
Number of Residues11
Detailsbinding site for residue 6KA A 302
ChainResidue
AGLY96
APHE97
AMET98
AMET103
AGLY104
APHE149
AMET161
AALA198
AMET199
AILE202
ANAD301

site_idAC3
Number of Residues22
Detailsbinding site for residue NAD B 301
ChainResidue
BGLY14
BILE15
BILE16
BSER20
BILE21
BPHE41
BLEU63
BASP64
BVAL65
BSER94
BILE95
BGLY96
BILE122
BMET147
BASP148
BPHE149
BLYS165
BPRO193
BILE194
BTHR196
B6KA302
BHOH401

site_idAC4
Number of Residues11
Detailsbinding site for residue 6KA B 302
ChainResidue
BGLY96
BPHE97
BMET98
BMET103
BGLY104
BALA157
BMET161
BALA198
BMET199
BILE202
BNAD301

site_idAC5
Number of Residues24
Detailsbinding site for residue NAD C 301
ChainResidue
CGLY14
CILE15
CILE16
CSER20
CILE21
CPHE41
CLEU63
CASP64
CVAL65
CSER94
CILE95
CGLY96
CILE122
CMET147
CASP148
CPHE149
CLYS165
CALA191
CPRO193
CILE194
CTHR196
C6KA302
CHOH402
CHOH407

site_idAC6
Number of Residues11
Detailsbinding site for residue 6KA C 302
ChainResidue
CLEU207
CNAD301
CGLY96
CPHE97
CMET98
CMET103
CGLY104
CMET161
CALA198
CMET199
CILE202

site_idAC7
Number of Residues22
Detailsbinding site for residue NAD D 301
ChainResidue
DGLY14
DILE15
DILE16
DSER20
DILE21
DPHE41
DLEU63
DASP64
DVAL65
DSER94
DILE95
DGLY96
DILE122
DMET147
DASP148
DPHE149
DLYS165
DPRO193
DILE194
DTHR196
D6KA302
DHOH401

site_idAC8
Number of Residues11
Detailsbinding site for residue 6KA D 302
ChainResidue
DGLY96
DPHE97
DMET98
DMET103
DGLY104
DALA157
DMET161
DALA198
DMET199
DILE202
DNAD301

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues20
DetailsBINDING: BINDING => ECO:0000269|PubMed:10336454, ECO:0000269|PubMed:16647717, ECO:0000269|PubMed:7886450, ECO:0007744|PDB:1BVR, ECO:0007744|PDB:1ENY, ECO:0007744|PDB:2AQ8
ChainResidueDetails
ASER20
BILE194
CSER20
CASP64
CILE95
CLYS165
CILE194
DSER20
DASP64
DILE95
DLYS165
AASP64
DILE194
AILE95
ALYS165
AILE194
BSER20
BASP64
BILE95
BLYS165

site_idSWS_FT_FI2
Number of Residues4
DetailsBINDING: BINDING => ECO:0000269|PubMed:10336454
ChainResidueDetails
ATYR158
BTYR158
CTYR158
DTYR158

site_idSWS_FT_FI3
Number of Residues4
DetailsSITE: May act as an intermediate that passes the hydride ion from NADH to the substrate => ECO:0000305|PubMed:10336454
ChainResidueDetails
APHE149
BPHE149
CPHE149
DPHE149

site_idSWS_FT_FI4
Number of Residues4
DetailsSITE: Transition state stabilizer => ECO:0000305|PubMed:10521269
ChainResidueDetails
ATYR158
BTYR158
CTYR158
DTYR158

site_idSWS_FT_FI5
Number of Residues4
DetailsMOD_RES: Phosphothreonine => ECO:0000269|PubMed:20864541, ECO:0000269|PubMed:21143326
ChainResidueDetails
ATHR266
BTHR266
CTHR266
DTHR266

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PDB entries from 2024-07-10

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